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The AC 2 peptide from Trapa japonica fruit helps protect hair cells and may treat hair loss.

Upadacitinib improved multiple immune-related conditions in one patient.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Upadacitinib improved symptoms and hair regrowth in a teen with multiple autoimmune conditions.

AHCC reduces hair loss and liver injury caused by chemotherapy in rodents.

HIF-1A may aid hair growth, Backhousia citriodora improves skin, autologous cells stabilize hair loss, infrared thermography assesses alopecia, and a new treatment preserves hair.

ECM1-modified stem cells can effectively treat liver cirrhosis.

Removing Mediator 1 causes teeth cells to turn into hair cells.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

The hydrogel with a 1:3 ratio of hydroxyethyl cellulose to hyaluronic acid is effective for delivering drugs through the skin to treat acne.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

TCHHL1 is a protein important for hair growth, found in hair follicles.

A specific DNA region controls skin cell gene expression by working with certain proteins.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The hedgehog signaling pathway is crucial for hair growth but not for the initial creation of hair follicles.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A mix of specific inhibitors and a growth factor helps keep hair growth cells from losing their properties in the lab.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

LSD1 is crucial for regenerating hair cells in zebrafish.

Mouse hair follicle stem cells have a flexible chromatin state that supports skin health and hair growth.

A protein called HIF-1a helps control hair growth genes and could be targeted to treat hair loss.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Blocking the enzyme 11β-HSD1 might help treat obesity and metabolic issues.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.